Biochemistry Department, Faculty of Science, Jeddah University, Jeddah 23235, Saudi Arabia.
Division of Cardiovascular & Diabetes Research, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM), University of Leeds, Leeds LS2 9JT, UK.
Int J Mol Sci. 2021 Mar 20;22(6):3170. doi: 10.3390/ijms22063170.
Hypofibrinolysis is a key abnormality in diabetes and contributes to the adverse vascular outcome in this population. Plasminogen activator inhibitor (PAI)-1 is an important regulator of the fibrinolytic process and levels of this antifibrinolytic protein are elevated in diabetes and insulin resistant states. This review describes both the physiological and pathological role of PAI-1 in health and disease, focusing on the mechanism of action as well as protein abnormalities in vascular disease with special focus on diabetes. Attempts at inhibiting protein function, using different techniques, are also discussed including direct and indirect interference with production as well as inhibition of protein function. Developing PAI-1 inhibitors represents an alternative approach to managing hypofibrinolysis by targeting the pathological abnormality rather than current practice that relies on profound inhibition of the cellular and/or acellular arms of coagulation, and which can be associated with increased bleeding events. The review offers up-to-date knowledge on the mechanisms of action of PAI-1 together with the role of altering protein function to improve hypofirbinolysis. Developing PAI-1 inhibitors may form for the basis of future new class of antithrombotic agents that reduce vascular complications in diabetes.
纤溶活性降低是糖尿病的一个主要异常,并导致该人群的血管不良结局。纤溶酶原激活物抑制剂-1(PAI-1)是纤维蛋白溶解过程的重要调节剂,在糖尿病和胰岛素抵抗状态下,这种抗纤维蛋白溶解蛋白的水平升高。本综述描述了 PAI-1 在健康和疾病中的生理和病理作用,重点介绍了作用机制以及血管疾病中的蛋白异常,特别关注糖尿病。还讨论了使用不同技术抑制蛋白功能的尝试,包括直接和间接干扰产生以及抑制蛋白功能。通过靶向病理异常而不是目前依赖于对凝血的细胞和/或无细胞部分的深度抑制的方法来开发 PAI-1 抑制剂,代表了管理纤溶活性降低的另一种方法,这可能与出血事件增加有关。该综述提供了关于 PAI-1 作用机制的最新知识,以及改变蛋白功能以改善纤溶活性降低的作用。开发 PAI-1 抑制剂可能为减少糖尿病血管并发症的新一代抗血栓药物奠定基础。